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Good Products will showcase its electronic document management solutions (EDMSs) at the Drug Information Association (DIA) 45th annual meeting in San Diego, California, on 21-25 June.

Good Products (booth 1,043), a provider of enterprise content management (ECM) solutions, has designed software to allow the pharmaceutical, biotechnology and life-science sectors to fully comply with regulations while increasing business efficiencies at a fraction of the cost of traditional content management systems.

The G-docs suite offers a regulatory-compliant solution for tracking document version history, managing approvals and monitoring and recording changes in an audit log.

Functional modules for the G-docs suite – such as Valman, G-SOPs and G-train – are intended to help organisations manage documents such as equipment validation and training records.

G-docs also offers PDF document rendering and digital signatures by Cosign.

A G-SOPs tool has recently been added to the G-docs portfolio, facilitating the creation, management and storage of controlled documents relating to standard operating procedures (SOPs) for use in the life-science industry.

G-SOPs also helps organisations to achieve full compliance with FDA 12 CFR part 11 guidelines and will be available for demonstration at the DIA show.

Good Products will also be highlighting its Clinical Technology Consulting division – designed to enable biopharmaceutical sponsors and CROs to optimise their use of clinical technology – at the DIA annual meeting.

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